Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
Phenotypes
Genetic Variation
Gene expression
Pathway
Molecular interactions
Regulation
External references
Supporting evidence
ID History
- Gene history

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Gene: NOD2 ENSBTAG00000020936

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Description

nucleotide binding oligomerization domain containing 2 [Source:VGNC Symbol;Acc:VGNC:32151]

Location

Primary_assembly 18: 19,090,037-19,119,730 forward strand.

ARS-UCD1.3:CM008185.2

About this gene

This gene has 2 transcripts (splice variants), 166 orthologues and 15 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSBTAT00000027887.6	NOD2-201	5104	1013aa	ENSBTAP00000027887.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A0H4JCB7 Q6E804	A single transcript chosen for a gene which is the most conserved, most highly expressed, has the longest coding sequence and is represented in other key resources, such as NCBI and UniProt. This is defined in detail on http://www.ensembl.org/info/genome/genebuild/canonical.htmlEnsembl Canonical, APPRIS P1: Transcript(s) expected to code for the main functional isoform based solely on the core modules in the APPRIS. APPRIS is a system to annotate alternatively spliced transcripts based on a range of computational methods to identify the most functionally important transcript(s) of a gene. APPRIS P1,
ENSBTAT00000086084.2	NOD2-202	5041	992aa	ENSBTAP00000069610.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A3Q1MEW2	-

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Summary

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